| Tag | Content |
|---|
EnhancerAtlas ID | HS133-16534 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr2:26240220-26241450 |
| | Number of super-enhancer constituents: 8 | ID | Coordinate | Tissue/cell |
| SE_09566 | chr2:26240304-26241810 | CD14 | | SE_26712 | chr2:26239870-26242089 | Esophagus | | SE_28420 | chr2:26240306-26241937 | Fetal_Intestine | | SE_29154 | chr2:26239992-26242119 | Fetal_Intestine_Large | | SE_32014 | chr2:26240172-26241573 | Gastric | | SE_35193 | chr2:26240079-26241982 | HeLa | | SE_36382 | chr2:26240216-26241937 | HMEC | | SE_64640 | chr2:26240168-26241940 | NHEK |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH02I026017 | chr2 | 26240097 | 26242426 |
|
Enhancer Sequence | CCATCCTCCG GCCTCAGCAT CCCAAAGTAC TGGGATTATA GGCATGCACC ACTGCACCAG 60
GCAAGGACAC AGATTTTTAT TGTTCACCCA CAAAGTGCTT CACATGCACT ACTTTGTCTG 120
ACCCTCACGA CAACCTGCAA GGTAGGTATT GTATTCCTAC TGTACGGATG AGAAAAACTG 180
AGACTCACAA AGGTTAGTTA CTAGCTCAAG ATCATGTATG CCTCAGTGGC AGGGCCAGGA 240
TTCAGAGCAG GGTGGCCTGG AGGTCTGAGG TTGGAAGCAG GTGTCACCTT AATGACTTAG 300
GAATGAGGTC AGTGTCTGTG TCCTCCAATT ATGGTGCCAG GCTCAGTCTC TACGAATGCC 360
TGGAGAATAT GTCAGCACTT ACTGTAGCTT CATGTTTAGG CCAAGAAAAG GCTGAGATGA 420
GATGATCCAT GAGAGTTTTT CACAGAAACA CAGACCAAAC ACAGAAGCAA AATCTTGGTC 480
TTCATATTGC CCCAGACTTG TTCTCTTCTG GGACTGAACC TAGTGTTAGA ATCCTGCTCT 540
GCAGGAATAG GGGGGTGTCT TTACATTTCA TTCTGGTTAT TTGCCTAAAG CAAATCCCAG 600
AGATACCCAG AGAGGGAAGA CTTTCCTCTG CAGATGGTGG AAGATGCTGG CGCCCAGGCC 660
ATCCTATGTC ATCTGTATCC AGACACAGAT TCCAGATCCC TGTTCATGCC TCTGAGGACA 720
TGGAGCGGGC CTTTTAGCTC TCTTCAGAGC TAGAGTTTCA GGCATATGGT TGCTGCCCTG 780
GATGACAAGG GTAGCACATG GGTGGGAACT CCAGATGCAT GTAAGGGAGC AAGAAGCTGC 840
CCACTGAGGA GAATGCTGGG ATAGTGCAGG GCTGGGCTGG CCCAACTAGT TCAGCTCAGC 900
CAGGAAAGGG CAGGTCAGAT CTGGCTCAGC AGGGGAGGCT GTGTCGGGGA GTGGTGCTGA 960
CTCAGGGCCT GGTGAGTCAG GTGACAGCCA AGGACAGCTG TTGCCTGGGT GTTTTTAGAA 1020
AACTTTGGCT GCCAACCACT CTCTCATGGG TGCTTCTGCA CCTACTCAGA AGCAGGCAGA 1080
AAAAAGGAGG GCATCTTCTG TATAAGAAGC TCTGGGTGAG GGGTATTAAT ATCTGGCTCT 1140
ACTTATGTTG ATCCTTCCCA TGAAGTACCT AGAAAACGGA GCAGAAATTA ATTGAGAGGC 1200
TTCCAAATCC CTTCTGAATT CTCTGAAAAT 1230
|
